K-number	K955077
Device name	ANTHOS 2010 READER
Applicant	Anthos Labtec, Inc.
Product code	JJQ
Device class	Class I
Decision date	Dec 4, 1995
Decision	Substantially Equivalent
Regulation	862.2300

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Source

View the full FDA submission: accessdata.fda.gov

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ANTHOS 2010 READER

Everything you need for a 510(k) submission. Nothing you don't.